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Compound Detail

CHEMBL197408

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COc1ccc(NC(=O)N2CCN(c3ccc(-c4ccccc4)cc3)CC2)cc1N1CCN(C)CC1
ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID CHEMBL197408
Phase Preclinical
Structure Type MOL
InChI Key WJYDVXOBGXFRGI-UHFFFAOYSA-N
6
Targets
6
Activities
1
Assay Types
0
PK Parameters
20
Publications
0
Known Names

Molecular Properties

485.6
MW (Da)
4.47
ALogP
5
HBA
1
HBD
51.3
PSA (Ų)
0.58
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H35N5O2
MW 485.63
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness -1.44

Activity Summary

Ki 6 meas. best 8.19

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2C
CHEMBL225
 Ki 8.19 8.19 6.5 1
5-hydroxytryptamine receptor 1B
CHEMBL1898
 Ki 7.86 7.86 13.7 1
5-hydroxytryptamine receptor 2A
CHEMBL224
 Ki 6.77 6.77 171.0 1
5-hydroxytryptamine receptor 1D
CHEMBL1983
 Ki 6.68 6.68 209.2 1
5-hydroxytryptamine receptor 1A
CHEMBL214
 Ki 6.39 6.39 405.0 1
5-hydroxytryptamine receptor 6
CHEMBL3371
 Ki 5.84 5.84 1429.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
5-hydroxytryptamine receptor 2C Ki = 6.5 nM 8.19 In vitro binding affinity towards cloned human 5-HT2C receptor using [3H]5-carbo... 16143528
5-hydroxytryptamine receptor 1B Ki = 13.7 nM 7.86 In vitro binding affinity towards cloned human 5-HT1B receptor using [3H]5-carbo... 16143528
5-hydroxytryptamine receptor 2A Ki = 171.0 nM 6.77 In vitro binding affinity towards cloned human 5-HT2A receptor using [3H]5-carbo... 16143528
5-hydroxytryptamine receptor 1D Ki = 209.2 nM 6.68 In vitro binding affinity towards cloned human 5-HT1D receptor using [3H]5-carbo... 16143528
5-hydroxytryptamine receptor 1A Ki = 405.0 nM 6.39 In vitro binding affinity towards cloned human 5-HT1A receptor using [3H]5-carbo... 16143528
5-hydroxytryptamine receptor 6 Ki = 1429.0 nM 5.84 In vitro binding affinity towards cloned human 5-HT6 receptor using [3H]5-carbox... 16143528

Literature References

PubMed DOI Target Context # Activities
16143528 10.1016/j.bmcl.2005.07.024 Muscarinic acetylcholine receptor M3 1
16143528 10.1016/j.bmcl.2005.07.024 D(2) dopamine receptor 1
16143528 10.1016/j.bmcl.2005.07.024 5-hydroxytryptamine receptor 7 1
16143528 10.1016/j.bmcl.2005.07.024 5-hydroxytryptamine receptor 6 1
16143528 10.1016/j.bmcl.2005.07.024 5-hydroxytryptamine receptor 2C 1
16143528 10.1016/j.bmcl.2005.07.024 5-hydroxytryptamine receptor 2A 1
16143528 10.1016/j.bmcl.2005.07.024 5-hydroxytryptamine receptor 1A 1
16143528 10.1016/j.bmcl.2005.07.024 Unchecked 1
16143528 10.1016/j.bmcl.2005.07.024 Muscarinic acetylcholine receptor M5 1
16143528 10.1016/j.bmcl.2005.07.024 Muscarinic acetylcholine receptor M4 1
16143528 10.1016/j.bmcl.2005.07.024 5-hydroxytryptamine receptor 1D 1
16143528 10.1016/j.bmcl.2005.07.024 5-hydroxytryptamine receptor 1B 1
16143528 10.1016/j.bmcl.2005.07.024 Muscarinic acetylcholine receptor M2 1
16143528 10.1016/j.bmcl.2005.07.024 Muscarinic acetylcholine receptor M1 1
16143528 10.1016/j.bmcl.2005.07.024 Histamine H1 receptor 1
16143528 10.1016/j.bmcl.2005.07.024 Mu-type opioid receptor 1
16143528 10.1016/j.bmcl.2005.07.024 Delta-type opioid receptor 1
16143528 10.1016/j.bmcl.2005.07.024 Kappa-type opioid receptor 1
16143528 10.1016/j.bmcl.2005.07.024 D(1B) dopamine receptor 1
16143528 10.1016/j.bmcl.2005.07.024 D(4) dopamine receptor 1

Data from ChEMBL 36 via Core Engine